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Found 1 matching solution for this experiment
pET-21b-VP24
Yunkun Wu, State Key Laboratory of Structural Chemistry, Fujian
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All recombinant plasmids were transformed into Escherichia coli BL21 (DE3) cells. Overexpression was performed by the induction of mid-log-phase E. coli BL21 (DE3) cells with 0.3 mM isopropyl β-d-1-thiogalactopyranoside (IPTG) for 12–16 h at 16°C. |
The overexpressed VP24-His6 was purified using Ni–NTA affinity chromatography (GE Healthcare) followed by gel filtration using Superdex 200 HR 16/60 (GE Healthcare) equilibrated in a buffer consisting of 25 mM Tris–HCl pH 7.0, 200 mM NaCl, 5% glycerol. |
Protocol tips |
All recombinant plasmids were transformed into Escherichia coli BL21 (DE3) cells. Overexpression was performed by the induction of mid-log-phase E. coli BL21 (DE3) cells with 0.3 mM isopropyl β-d-1-thiogalactopyranoside (IPTG) for 12–16 h at 16°C. |
Downstream tips |
The overexpressed VP24-His6 was purified using Ni–NTA affinity chromatography (GE Healthcare) followed by gel filtration using Superdex 200 HR 16/60 (GE Healthcare) equilibrated in a buffer consisting of 25 mM Tris–HCl pH 7.0, 200 mM NaCl, 5% glycerol. |
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